EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS064-07265 
Organism
Homo sapiens 
Tissue/cell
GM18507 
Coordinate
chr19:7185490-7186830 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11670972chr197185591hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:7185903-7185921GGAAGGAAGGAAAAAAAA+6.18
EWSR1-FLI1MA0149.1chr19:7185895-7185913AAAAGGAAGGAAGGAAGG+7.95
EWSR1-FLI1MA0149.1chr19:7185899-7185917GGAAGGAAGGAAGGAAAA+9.07
IRF1MA0050.2chr19:7186206-7186227AAACAAAAAATGAAACAAAAC-6.78
IRF1MA0050.2chr19:7186690-7186711TTTTACTTTCTTTTTCTTTTC+7.71
IRF9MA0653.1chr19:7186620-7186635AACCAAACTGAAACT+6.61
POU2F2MA0507.1chr19:7185559-7185572ACATGCAAATGTG-6
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1971855447185600
Number: 1             
IDChromosomeStartEnd
GH19I007185chr1971858687187067
Enhancer Sequence
AAAAAAGTGG CTGCAGATCC TGCCTTTGGG AGCACAAGGT CTAATGGAGG AGACATGTTA 60
GTTACTTAAA CATGCAAATG TGGCTCGGTG TGGTGGCTCA CGCCTGTAAT CCTAGCAATT 120
TGGGAGGTCG AGGCGGGTGG ATCACCTGAG GTCAGGAGTT TGAGACCAGC CTGGTCAACA 180
TGGTGAAACC CTGTCTCTAC TAAAAATACA AAAATTAGCT AGGTGTGCTG GTGCATGCCT 240
GTAATCCCAG CTGCTCAGGA GGCTGAGGCA CGAGAATCAC TTGAATCTGG GAGGTGGAGG 300
CTGCAGTGAG CCATGATCGT GCCACTATAC TCCAGCCTGG GCAACAAGTG CAAAATTCTG 360
TCAAAAAAAA AAAAAAAAAA GAGAGAGAGA GACAAAGAGA GAGAGAAAAG GAAGGAAGGA 420
AGGAAAAAAA AAAGGCTGGT TGTGGTGGCT CATGCCTGTA ATCCTAGCAC TTTGGGAGGC 480
CAAGGTGGGC GGATCACCTG AGGTCAGGAG TTTCAGACCA GCCTGGCCAA CATGGTGAAA 540
CCCCATCTCT ACTGATGATA CAAACAATTA GCCGGGTGTG GTGGTGGGCG TCTGTAATCC 600
CAGCTACTCA GGAGGCTGAG GCAGGAGAAT CGCTTGAACC TGGGAGGGGA GGTTGCAGGG 660
AGCCGAGATC ATGCCACTGC ACTCCAGCCT TGGTGACAGA GGGAGACTCT GTCTCAAAAC 720
AAAAAATGAA ACAAAACAAA AAATAAGAAA GAAAGTTGGG GAGTGTTCTT CACCCCAAAT 780
CCCCAGACTG TGATTCTCAG CACAGTGGAT CCCACCGGCC AAACTCAGGG AACAGAAGTG 840
GCCCCAGAAG CTACATCCAT ATATGAACAG CACCATCTGG TCGAAATTTC TGCGATGACG 900
GAAATGTTCT CTATCTGGGC CATCCAACAT AGTAGCCACT TCTCCCCTGT GGCTTCTGAA 960
TGTGCTTAGT GCAACTAGGA AATCCAATTT TTTTTTTAAT TGTGGTAAAA TACACATAGC 1020
ATAAAATTCA CCATTGTAAT CATGTTTAAA TGTATAGTTC AGTGGTATTA AATACTTTTA 1080
TGTGGCTATG CAACCATCAC CACCACCCAT CTCCAGAACT TTCTCACCTT AACCAAACTG 1140
AAACTCTGCC CCCATGAAAC AGTCACACTC ATCCTCCTCC CCAACTCCTG GCACCTGCCA 1200
TTTTACTTTC TTTTTCTTTT CTTTTTTTTT ATTTTTATTT TTTGAGATGG AGTCTTGCTT 1260
TGTTGCCCAG GCTGGGGTGC AGTGGCGCGA TCTCAGCTCA CTGTAACCTC TGCCTCCCGG 1320
GTTCAAGTGA TTCTCCTGCC 1340